Disease #00010

Official abbreviation	615228
Name	Mitochondrial complex (ATP synthase) deficiency, nuclear type 4, 615228 (3)
OMIM ID	615228
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 2 genes	ATP5A1, ATP5F1A
Associated tissues	-
Disease features	-
Remarks	-